Anti-inflammatory and antialgic actions of a nanoemulsion of Rosmarinus officinalis L. essential oil and a molecular docking study of its major chemical constituents

被引:0
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作者
Raphaelle Sousa Borges
Emerson Silva Lima
Hady Keita
Irlon Maciel Ferreira
Caio Pinho Fernandes
Rodrigo Alves Soares Cruz
Jonatas Lobato Duarte
Josué Velázquez-Moyado
Brenda Lorena Sánchez Ortiz
Andrés Navarrete Castro
Jaderson Vieira Ferreira
Lorane Izabel da Silva Hage-Melim
José Carlos Tavares Carvalho
机构
[1] Universidade Federal do Amapá (UNIFAP),Laboratório de Pesquisa em Fármacos, Departamento de Ciências Biológicas e Saúde
[2] Universidade Federal do Amazonas,Laboratório de Atividade Biológica – BIOPHAR
[3] Avenida General Rodrigo Otávio,Laboratório de Nanotecnologia Fitofarmacêutica, Departamento de Ciências Biológicas e Saúde
[4] Universidad Tecnologica del Valle de Toluca,Laboratório de Farmacologia de Productos Naturales (LFPN), Facultat de Química
[5] Universidade Federal do Amapá (UNIFAP),Laboratório de Química Farmacêutica e Medicinal (PharMedChem), Departamento de Ciências Biológicas e Saúde
[6] Universidad Nacional Autônoma de México (UNAM),Programa de Pós
[7] Ciudad Universitária,Graduação em Inovação Farmacêutica, Curso de Farmácia, Departamento de Ciências Biológicas e Saúde
[8] Universidade Federal do Amapá (UNIFAP),undefined
[9] Universidade Federal do Amapá (UNIFAP),undefined
来源
Inflammopharmacology | 2018年 / 26卷
关键词
Nanoemulsions; H; S; Anti-inflammatory; Antialgic; Molecular docking;
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学科分类号
摘要
We evaluate the anti-inflammatory and antialgic potency of a nanoemulsion (NEORO) containing the essential oil of Rosmarinus officinalis L. (EORO), which is composed primarily of limonene, camphor and 1,8-cineole. The EORO and NEORO were administered orally 30 min prior to starting the experiments. In a test of rat paw oedema induced by carrageenan, NEORO was effective in doses of 498 µg/kg, and it inhibited 46% of the maximum peak of the oedema; in a dose of 300 mg/kg, EORO inhibited 50% of the maximum peak of the oedema. In an acetic acid-induced writhing test, NEORO yielded a dose-dependent effect, and a dose of 830 µg/kg inhibited 84% of the algesic process; a dose of 100 mg/kg of EORO inhibited 55%. In an assay for H2S production in rat stomachs, a dose of 498 µg/kg of NEORO inhibited H2S production in all of the measurement phases, and a dose of 100 mg/kg EORO inhibited 60% and influenced the effect of the ethanol significantly, reducing the production of H2S. We suggest that NEORO potentiated the effect of EORO, demonstrating effectiveness in doses 600 times lower than those applied with EORO. Among the major compounds of EORO, the camphor molecule exhibited the largest number of interactions with the therapeutic targets related to the inflammatory process, suggesting that it is responsible for EORO’s anti-inflammatory and antialgic effects. This work paves the way for future investigations related to the therapeutic role of NEORO in the inflammation process.
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页码:183 / 195
页数:12
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